Canonical Allele Identifier: CA1702658905

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41961672T= , CM000669.2:g.41961672T=	GRCh38
NC_000007.13:g.42001270T= , CM000669.1:g.42001270T=	GRCh37
NC_000007.12:g.41967795T=	NCBI36
NG_008434.1:g.280349A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*2658A= MANE Select	ENSP00000379258.3:n.*2658A=
ENST00000677288.1:c.*2658A=	ENSP00000503986.1:n.*2658A=
ENST00000677605.1:c.*2658A=	ENSP00000503743.1:n.*2658A=
ENST00000678429.1:c.*2658A=	ENSP00000502957.1:n.*2658A=
ENST00000395925.7:c.*2658A=	ENSP00000379258.3:n.*2658A=
NM_000168.5:c.*2658A=	NP_000159.3:n.*2658A=
XM_005249703.1:c.*2658A=	XP_005249760.1:n.*2658A=
XM_005249704.2:c.*2658A=	XP_005249761.1:n.*2658A=
XM_011515272.1:c.*2658A=	XP_011513574.1:n.*2658A=
XM_011515273.1:c.*2658A=	XP_011513575.1:n.*2658A=
XM_011515274.1:c.*2658A=	XP_011513576.1:n.*2658A=
NM_000168.6:c.*2658A= MANE Select	NP_000159.3:n.*2658A=